ABCC8 p.Trp898Cys
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PMID: 17213273
[PubMed]
Stanik J et al: "Prevalence of permanent neonatal diabetes in Slovakia and successful replacement of insulin with sulfonylurea therapy in KCNJ11 and ABCC8 mutation carriers."
No.
Sentence
Comment
97
In 2002, he was diagnosed with the Wolcott-Rallison syndrome with mutations in the EIF2AK3 gene (compound heterozygous for W898C and L1057P mutations) (29).
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ABCC8 p.Trp898Cys 17213273:97:123
status: NEW